A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7466n54



Internal ID20140890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14687597..15014697hg38UCSC Ensembl
chr20:14668243..14995343hg19UCSC Ensembl
chr20:14616243..14943343hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38327101
hg19327101
hg18327101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585467, nsv585456
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7466n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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